Latest Drug Development jobs in New Jersey - JobisJob United States Mobile

159 Drug Development Jobs in New Jersey

Senior Regulatory Affairs Associate Breckenridge Pharmaceutical, Inc. - Berkeley Heights, NJ, United States in drug development from early stage development through final formulation, ensuring compliance with principles of Quality-by-Design, cGMP, and FDA rules and regulations Support new product launches 5 days ago
Trial Supplies Manager Ivory Systems - Summit, NJ, United States Meetings as required. • Traveling as required (<10%). • Writing of / input to departmental SOPs. • Performs other tasks as assigned. Required: • Moderate / Strong knowledge of the global drug development 6 days ago
Senior Director, Drug Development, Project Management - Rare Diseases (Pompe Disease) Shionogi Inc. - Florham Park, New Jersey Overview: The Senior Director of Drug Development Project Management is accountable for providing project management and drug development expertise to global project teams within the rare diseases 4 days ago
Analytical Chemist Ivory Systems - Hopewell, NJ, United States methods, and reports. Perform routine analytical tests (e.g., SEC, CE, ICIEF, Protein A) to support the upstream and downstream process development. • Support the development and transfer of analytical 6 days ago
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Business Analyst SSi People - Princeton, NJ, United States of solutions. Qualifications & Experience Bachelor’s degree in science or technology. Basic understanding of drug development and major clinical systems is required. Foundational understanding of key business 7 days ago
Director, Data Science Neuroscience, Real World Evidence Johnson & Johnson - Titusville, NJ and external cross-functional talent. This role requires experience in pharmaceutical drug development and knowledge of sophisticated analytics, bringing to bear diverse data domains and using artificial USD 157,000.00 - 271,400.00 per year 4 days ago
Analytical Development Analyst Randstad Life Sciences US - Hopewell, NJ, United States process development. Support the development and transfer of analytical methods of biologics drugs (including monoclonal antibodies, bispecific antibodies, ADC). Understand CMC process of biologics drugs 6 days ago
Director, Regulatory Affairs Strategy SciPro - , NJ, United States for specific assets within Oncology. The position will report directly into the VP of Regulatory Affairs. The company is growing exponentially with a focus in drug development within the oncology space 7 days ago
Scientific - Global Regulatory CMC Manager TechDigital Corporation - Summit, New Jersey (IND/CTAs, BLA/NDAs, MAAs, responses, variations and briefing documents) Knowledge of FDA, EMA and/or ICH guidelines and CMC regulations Experience in drug development processes and post-approval 13 days ago
Business Analyst-clinical operations (Hybrid) Rangam - Lawrenceville, NJ, United States of solutions. Qualifications & Experience Bachelor’s degree in science or technology. Basic understanding of drug development and major clinical systems is required. Foundational understanding of key business 7 days ago

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